FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
MONARCH II IOL DELIVERY SYSTEM
K Number: K001157
·
Decision Jun 27, 2000
Classifications
1
FEI Numbers
40
Registration Numbers
40
Same Product Code
38
Applicant Total
14
Review Days
78
Basic Information
- Device Name
- MONARCH II IOL DELIVERY SYSTEM
- K Number
- K001157
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 886.4300
- Medical Specialty
- Ophthalmic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- ALCON RESEARCH, LTD.
- Date Received
- April 10, 2000
- Decision Date
- June 27, 2000
- Product Code
- KYB
- Advisory Committee
- Ophthalmic
- Review Advisory Committee
- OP
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| KYB | Lens, Guide, Intraocular | FDA class 1 | Ophthalmic |
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